Certain 7-(2-substituted benzoyl)-1-heterospiro-(4,5)decane-(6,8)-diones

ABSTRACT

Compounds of the formula ##STR1## wherein X is oxy, thio, sulfinyl or sulonyl; 
     R is halogen; C 1  -C 2  alkyl; C 1  -C 2  alkoxy; trifluoromethoxy; difluoromethoxy; nitro;cyano; C 1  -C 2  haloalkyl; R a  SO n  -- wherein n is 0 or 2 and R a  is C 1  -C 2  alkyl, trifluoromethyl or difluoromethyl; 
     R 1  is hydrogen, C 1  -C 4  alkyl, phenyl or substituted phenyl; 
     R 2  is hydrogen or C 1  -C 4  alkyl; or 
     R 1  and R 2  together are C 2  -C 5  alkylene; 
     R 3  is hydrogen, C 1  -C 4  alkyl, phenyl or substituted phenyl with the proviso that R 1  and R 3  are not both phenyl or substituted phenyl; 
     R 4  is hydrogen or C 1  -C 4  alkyl; and 
     R 5  and R 6  independently are (1) hydrogen; (2) halogen; (3) C 1  -C 4  alkyl; (4) C 1  -C 4  alkoxy; (5) trifluoromethoxy; (6) cyano; (7) nitro; (8) C 1  -C 4  aloalkyl; (9) R b  SO n  -- wherein n is the integer 0, 1 or 2; and R b  is (a) C 1  -C 4  alkyl; (b) C 1  -C 4  alkyl substituted with halogen or cyano; (c) phenyl; or (d) benzyl; (10) --NR c  R d  wherein R c  and R d  independently are hydrogen or C 1  -C 4  alkyl; (11) R e  C(O)-- wherein R e  is C 1  -C 4  alkyl or C 1  -C 4  alkoxy; or (12) --SO 2  NR c  R d  wherein R c  and R d  are as defined; and (13) --N(R c )C(O)R d  wherein R c  and R d  are as defined; and their salts.

BACKGROUND OF THE INVENTION

European patent application No. 0 268 795 relates to certain herbicidal compounds that have the structural formula ##STR2## wherein R through R⁶ are substantially as defined below; R⁷ is hydrogen or alkyl; X is oxy, thio, sulfinyl or sulfonyl; and R⁸ is hydrogen, alkyl, haloalkyl or phenyl.

DESCRIPTION OF THE INVENTION

This invention relates to 7-(2-substituted benzoyl)-1-heterospiro[4.5]decane-6,8-diones and their use as herbicides.

One embodiment of this invention is an herbicidal composition comprising an herbicidally active 7-(2-substituted benzoyl)-1-(oxa or thia)spiro[4.5]decane-6,8-dione (or the 1-oxide or 1,1-dioxide derivative of the thia compound) and an inert carrier therefor. The 9- and 10-positions of the 1-heterospiro[4.5]decane-6,8-dione moiety are preferably substituted with groups hereinafter defined, most preferably with hydrogen or methyl groups. The substituted benzoyl moiety can be further substituted, preferably with the groups hereinafter recited.

Also embodied within the scope of this invention are novel compounds having the following structural formula ##STR3## wherein

X is oxy, thio, sulfinyl or sulfonyl;

R is halogen, preferably chlorine or bromine; C₁ -C₂ alkyl, preferably methyl; C₁ -C₂ alkoxy, preferably methoxy; trifluoromethoxy; difluoromethoxy; nitro; cyano; C₁ -C₂ haloalkyl, preferably trifluoromethyl; R^(a) SO_(n) - wherein n is 0 or 2, preferably 2 and R^(a) is C₁ -C₂ alkyl, preferably methyl, trifluoromethyl or difluoromethyl. Preferably, R is chlorine, bromine, C₁ -C₂ alkyl, C₁ -C₂ alkoxy, trifluoromethyl, cyano, nitro, C₁ -C₂ alkylthio or C₁ -C₂ alkylsulfonyl; more preferably chlorine, nitro, methyl, trifluoromethyl or methylsulfonyl;

R¹ is hydrogen; C₁ -C₄ alkyl, preferably methyl; phenyl; or substituted phenyl;

R² is hydrogen or C₁ -C₄ alkyl, preferably methyl; or

R¹ and R² together are C₂ -C₅ alkylene;

R³ is hydrogen; C₁ -C₄ alkyl, preferably methyl; phenyl; or substituted phenyl with the proviso that R¹ and R³ are not both phenyl or substituted phenyl;

R⁴ is hydrogen or C₁ -C₄ alkyl, preferably methyl; and

R⁵ and R⁶ independently are (1) hydrogen; (2) halogen, preferably chlorine, fluorine or bromine; (3) C₁ -C₄ alkyl, preferably methyl; (4) C₁ -C₄ alkoxy, preferably methoxy; (5) trifluoromethoxy; (6) cyano; (7) nitro; (8) C₁ -C₄ haloalkyl, more preferably trifluoromethyl; (9) R^(b) SO_(n) -wherein n is the integer 0, 1 or 2, preferably 2; and R^(b) is

(a) C₁ -C₄ alkyl, preferably methyl;

(b) C₁ -C₄ alkyl substituted with halogen or cyano, preferably chloromethyl, trifluoromethyl or cyanomethyl;

(c) phenyl; or

(d) benzyl;

(10) --NR^(c) R^(d) wherein R^(c) and R^(d) independently are hydrogen or C₁ -C₄ alkyl; (11) R^(e) C(O)-- wherein R^(e) is C₁ -C₄ alkyl or C₁ -C₄ alkoxy; (12) --SO₂ NR^(c) R^(d) wherein R^(c) and R^(d) are as defined; or (13) --N(R^(c))C(O)R^(d) wherein R^(c) and R^(d) are as defined.

Preferably R⁵ is in the 3-position. More preferably R⁵ is hydrogen, chlorine, fluorine, trifluoromethyl, cyano, C₁ -C₄ alkoxy or C₁ -C₄ thioalkyl. Most preferably, R⁵ is hydrogen. Preferably R⁶ is in the 4-position. Most preferably R⁶ is halogen, cyano, trifluoromethyl, or R^(b) SO₂ wherein R^(b) is C₁ -C₄ alkyl, preferably methyl or C₁ -C₄ haloalkyl, preferably chloromethyl, difluoromethyl or trifluoromethyl.

The term "C₁ -C₄ alkyl" includes methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl and t-butyl. The term "halogen" includes chlorine, bromine, iodine and fluorine. The terms "C₁ -C₄ alkoxy" includes methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, sec-butoxy, isobutoxy and t-butoxy. The term "C₁ -C₄ haloalkyl" includes the alkyl groups defined above under C₁ -C₄ alkyl in which one or more hydrogens is replaced by chlorine, bromine, iodine or fluorine.

Salts of the above-described compounds (as defined hereinafter) are included within the scope of this invention.

The compounds of this invention can have the following four structural formulae because of tautomerism: ##STR4## wherein R, R¹, R², R³, R⁴, R⁵ and R⁶ and X are as defined above.

The circled proton on each of the four tautomers is reasonably labile. These protons are acidic and can be removed by reaction with a base to form a salt having an anion of the following four resonance forms: ##STR5## wherein R, R¹, R², R³, R⁴, R⁵ and R⁶ and X are as defined above.

Examples of cations of these bases are inorganic cations such as alkali metals, e.g. lithium, sodium and potassium; the alkaline earth metals, e.g. calcium and magnesium or ammonium or organic cations such as substituted ammonium, sulfonium, sulfoxonium or phosphonium wherein the substitutents are aliphatic or aromatic groups.

Those skilled in the art will recognize in considering the salts of this invention that varying degrees of association between the anion and cation will exist depending upon the nature of the cation. In some instances with a suitable cation, such as copper, the salt can exist in a chelated form.

The compounds of this invention and their salts are active herbicides of a general type. That is, they are herbicidally effective against a wide range of plant species. The method of controlling undersirable vegetation of the present invention comprises applying an herbicidally effective amount of the above-described compounds or their salts to the area where control is desired.

The compounds of the present invention can be prepared by the following two-, or, if necessary, a three-step general method.

The process proceeds via the production of an enol ester intermediate as shown in reaction (1). The final product is obtained by rearrangement of the enol ester as shown in reaction (2), or, if necessary, by subsequent oxidation of the product obtained in step (2) as shown in reaction (3).

The process is conducted in the presence of a catalytic amount of a source of cyanide anion and/or hydrogen cyanide, together with a molar excess, with respect to the enol ester, of a moderate base.

The two reactions may be conducted as separate steps by isolation and recovery of the enol ester using conventional techniques prior to conducting step (2), or by addition of a cyanide source to the reaction medium after the formation of the enol ester, or in one step by inclusion of the cyanide sourc at the start of reaction (1). ##STR6## wherein R through R⁶ and X and moderate base are as defined and Y is halogen, preferably chlorine, C₁ -C₄ alkyl--C(O)--O--, C₁ -C₄ alkoxy--C(O)--O-- or ##STR7## wherein R, R⁵ and R⁶ in this portion of the molecule are identical with those in the reactant shown above and the moderate base is as defined, preferably tri-C₁ -C₆ alkylamine, alkali metal carbonate or alkali metal phosphate.

Generally, in step (1) mole amounts of the dione and substituted benzoyl reactant are used, along with a mole amount or excess of the base. The two reactants are combined in an organic solvent such as methylene chloride, toluene, ethyl acetate or dimethylformamide. The base or benzoyl reactant preferably is added to the reaction mixture with cooling. The mixture is stirred at 0° C.-50° C. until the reaction is substantially complete. ##STR8## wherein the moderate base and R through R⁶ and X are as defined above.

Generally, in step (2) a mole of the enol ester intermediate is reacted with 1 to 4 moles of the moderate base, preferably about 2 moles of moderate base and from 0.01 mole to about 0.5 mole or higher, preferably about 0.01-0.1 mole of the cyanide source. The mixture is stirred in a reaction pot until the rearrangement is substantially complete at a temperature below 50° C., preferably about 20° C. to about 40° C., and the desired product is recovered by conventional techniques.

Alternatively, certain compounds of this invention can be prepared by the following reaction: ##STR9## wherein R through R⁶ are as defined, m is the integer 1 or 2 and [O] is an oxidizing agent, preferably a peroxide such as peracetic acid or m-chloroperbenzoic acid.

Generally, in reaction step (3) the substituted thio is dissolved in methylene chloride and an oxidizing agent such as m-chloroperbenzoic acid (1.1 or 2.2 equivalents) is added portionwise and the reaction mixture is stirred for 1 to 8 hours. The product may be isolated using conventional techniques.

The term "cyanide source" refers to a substance or substances which under the rearrangement conditions consists of or generates hydrogen cyanide and/or cyanide anion.

Preferred cyanide sources are alkali metal cyanides such as sodium and potassium cyanide; cyanohydrins of methyl alkyl ketones having from 1-4 carbon atoms in the alkyl groups, such as acetone or methyl isobutyl ketone cyanohydrins; benzaldehyde cyanohydrin; cyanohydrins of C₂ -C₅ aliphatic aldehydes such as acetaldehyde cyanohydrin, propionaldehyde cyanohydrin, etc.; cyclohexanone cyanohydrin; lactonitrile; zinc cyanide; di- and tri-(lower alkyl) silyl cyanides, notably dimethyl- and trimethylsilyl cyanide; potassium ferric cyanide; and hydrogen cyanide itself. Hydrogen cyanide is considered most advantageous as it produces relatively rapid reaction and is inexpensive. Among cyanohydrins the preferred cyanide source is acetone cyanohydrin.

The cyanide source is used in an amount up to about 50 mole percent based on the enol ester. It may be used in as little as about 1 mole percent to produce an acceptable rate of reaction at about 40° C. on a small scale. Larger scale reactions give more reproducible results with slightly higher catalyst levels of about 2 mole percent. Generally about 1-10 mole % of the cyanide source is preferred.

The process is conducted with a molar excess, with respect to the enol ester, of a moderate base. By the term "moderate base" is meant a substance which acts as a base yet whose strength or activity as a base lies between that of strong bases such as hydroxides (which could cause hydrolysis of the enol ester) and that of weak bases such as N,N-dimethylaniline (which would not function effectively). Moderate bases suitable for use in this embodiment include both organic bases, e.g., trialkylamines such as triethylamine and inorganic bases such as alkali metal carbonates and phosphates. Suitable inorganic bases include potassium carbonate and trisodium phosphate.

The base is used in an amount of from about 1 to about 4 moles per mole of enol ester, preferably about 2 moles per mole.

When the cyanide source is an alkali metal cyanide, particularly potassium cyanide, a phase transfer catalyst may be included in the reaction. Particularly suitable phase transfer catalysts are the crown ethers.

A number of different solvents are useful in this process, depending on the nature of the acid halide or the acylated product. A preferred solvent for this reaction is 1,2-dichloroethane. Other solvents which may be employed, depending on the reactants or products include toluene, acetonitrile, methylene chloride, ethyl acetate, dimethylformamide, and methyl isobutyl ketone (MIBK).

In general, depending on the nature of the reactants and the cyanide source, the rearrangment may be conducted at temperatures up to about 50° C.

The above described substituted benzoyl chlorides can be prepared from the corresponding substituted benzoic acids according to the teaching of Reagents for Organic Synthesis, Vol. I, L. F. Fieser and M. Fieser, pp. 767-769 (1967). ##STR10## wherein R, R⁵ and R⁶ are as previously defined.

The substituted benzoic acids can be prepared by a wide variety of general methods according to the teaching of The Chemistry of Carboxylic Acids and Esters, S. Patai, editor, J. Wiley and Sons, New York, N.Y. (1969) and Survey of Organic Synthesis, C. A. Buehler and D. F. Pearson, J. Wiley and Sons, (1970).

The following are three representative examples of the methods described therein. ##STR11## wherein R, R⁵ and R⁶ are as previously defined.

In reaction (a) the substituted benzonitrile is heated to reflux in aqueous sulfuric acid for several hours. The mixture is cooled and the reaction product is isolated by conventional techniques. ##STR12## wherein R, R⁵ and R⁶ are as previously defined.

In reaction (b) the substituted acetophenone is heated to reflux for several hours in an aqueous hypochlorite solution. The mixture is cooled and the reaction product is isolated by conventional techniques. ##STR13## wherein R, R⁵ and R⁶ are as previously defined.

In reaction (c) the substituted toluene is heated to reflux in an aqueous solution of potassium permanganate for several hours. The solution is then filtered and the reaction product is isolated by conventional techniques.

The substituted 1-heterospiro[4.5]decane-6,8-diones can be prepared via reaction of a substituted acrylate with 2-acetyltetrahydrofuran or 2-acetyltetrahydrothiophene in a solvent such as toluene in the presence of a molar equivalent of a base such as sodium ethoxide. ##STR14## wherein R¹ through R⁴ and X are as defined above.

The 2-acetyltetrahydrofuran and -thiophene are obtained by reaction of the corresponding known acids with two mole equivalents of methyl lithium according to the teachings of M. J. Jorgensen, Organic Reactions, 18, 1 (1970). ##STR15## wherein X is defined above.

EXAMPLE 1 7-(2-Nitro-4-trifluoromethylbenzoyl)-1-thiaspiro[4.5]decane-6,8-dione ##STR16##

1-Thiaspiro[4.5]decane-6,8-dione [5.0 grams (g), 27 millimole (mmol)] and 2-nitro-4-trifluoromethylbenzoyl chloride (6.9 g, 27 mmol) were dissolved in 75 milliliters (ml) of methylene chloride at room temperature. Triethylamine (5.4 g, 54 mmol) was slowly added with cooling. The reaction mixture was stirred at room temperature for 5 hours and then poured into 2 normal (N) hydrochloric acid. The aqueous phase was discarded and the organic phase was dried over magnesium sulfate and then evaporated under vacuum to yield the intermediate enol ester. The enol ester was dissolved in 75 ml of acetonitrile, and triethylamine (5.4 g, 54 mmol) and acetone cyanohydrin (0.41 g, 5 mmol) were added. The reaction mixture was stirred at room temperature for 5 hours and then concentrated in vacuo. The residual gum was then partitioned between methylene chloride (150 ml) and 2N hydrochloric acid (100 ml). The methylene chloride layer was then washed with 5 percent (%) copper acetate, 5% potassium carbonate, 2N hydrochloric acid, and water. After drying over anhydrous magnesium sulfate, the methylene chloride solution was concentrated in vacuo to afford 3.6 g of the desired product as a viscous oil. The structure was confirmed by nuclear magnetic spectroscopy, infrared spectroscopy and mass spectroscopy.

EXAMPLE 2 7-(2-Nitro-4-trifluoromethylbenzoyl)-1-thiaspiro[4.5]decane-6,8-dione-1,1-dioxide ##STR17##

7-(2-Nitro-4-trifluoromethylbenzoyl)-1-thiaspiro[4.5]decane-6,8-dione (2.1 g, 5 mmol) was dissolved in methylene chloride (50 ml). Peracetic acid (40% in acetic acid, 2 g, 10 mmol) was added portion-wise to the stirred solution at room temperature, the reaction mixture was diluted with additional methylene chloride (100 ml) and washed with water (4 times (×) with 50 ml) and brine (1×50 ml). After drying over anhydrous magnesium sulfate, the methylene chloride solution was concentrated in vacuo to afford 2.0 g of the desired product as a viscous oil. The structure was confirmed by nuclear magnetic spectroscopy, infrared spectroscopy and mass spectroscopy.

The following is a table of certain selected compounds that are preparable according to the procedures described herein. Compound numbers are assigned to each compound and are used throughout the remainder of the application.

                  TABLE I                                                          ______________________________________                                          ##STR18##                                                                     Cmpd.                                                                          No.    R       R.sup.1                                                                              R.sup.2                                                                            R.sup.3                                                                            R.sup.4                                                                            X    R.sup.5                                                                             R.sup.6                             ______________________________________                                         1      NO.sub.2                                                                               H     H   H   H   S    H    H                                   2      NO.sub.2                                                                               H     H   H   H   SO.sub.2                                                                            H    H                                   3      Cl      H     H   H   H   O    H    4-SO.sub.2 CH.sub.3                 4      Cl      H     H   H   H   S    H    4-SO.sub.2 CH.sub.3                 5      Cl      H     H   H   H   SO.sub.2                                                                            H    4-SO.sub.2 CH.sub.3                 6      NO.sub.2                                                                               H     H   H   H   O    H    H                                   7      NO.sub.2                                                                               H     H   H   H   O    H    4-CF.sub.3                          8.sup.a                                                                               NO.sub.2                                                                               H     H   H   H   S    H    4-CF.sub. 3                         9.sup.b                                                                               NO.sub.2                                                                               H     H   H   H   SO.sub.2                                                                            H    4-CF.sub.3                          10     NO.sub.2                                                                               H     H   H   H   O    H    4-SO.sub.2 CH.sub.2 Cl              11     NO.sub.2                                                                               H     H   H   H   S    H    4-SO.sub.2 CH.sub.2 Cl              12     NO.sub.2                                                                               H     H   H   H   SO.sub.2                                                                            H    4-SO.sub.2 CH.sub.2 Cl              ______________________________________                                          .sup.a Prepared in Example 1.                                                  .sup.b Prepared in Example 2.                                            

The following Table shows the instrumental analysis spectral data for the compounds of Table I.

                  TABLE I-A                                                        ______________________________________                                         Compound                                                                       Number  Spectral Data                                                          ______________________________________                                         1       H-NMR (CDCl.sub.3): δ 1.50 (m, 1H), 2.01 (m, 1H),                        2.14 (m, 2H), 2.33 (m, 1H) 2.50 (m, 1H), 2.75                                  (m, 1H), 2.88 (m, 2H), 3.13 (m, 1H), 7.26 (d, 1H),                             2.88 (m, 2H), 3.13 (m, H), 7.26 (d, 1H), 7.58                                  (t, 1H), 7.71 (t, 1H), 8.22 (d, 1H), 16.60 (s, 1H)                             IR (film): υ (cm.sup.-1), 3060, 2940, 2860, 1680,                      1580, 1530, 1420, 1355, 865, 820, 795, 760, 740,                               710                                                                            MS (m/z): 51, 77, 100, 113, 140, 150, 186, 212,                                227, 253, 287, 333 (M.sup.+)                                           2       H-NMR (DMSO-d.sub.6), δ 1.76 (m, 1H), 1.95 (m, 2H),                      2.25-2.60 (m, 3H), 2.84 (m, 1H), 2.92-3.30                                     (m, 3H), 7.42 (d, 1H), 7.73 (t, 1H), 7.82 (t, 1H),                             8.22 (d, 1H)                                                                   IR (KBr pellet): υ (cm.sup.-1), 3110, 2950, 2910,                      2860, 1675, 1600, 1565, 1520, 1415, 1350, 1300,                                1150, 1120, 950, 855, 810, 790, 755, 700                                       MS (m/z): 51, 65, 77, 92, 104, 121, 133, 150, 158,                             186, 197, 213, 225, 227, 239, 251, 254, 301, 319                               (M.sup.+ - NO.sub.2)                                                   3       H-NMR (CDCl.sub.3): δ 1.63 (m, 1H), 1.96-2.36                            (m, 5H), 2.65-3.20 (m, 2H), 3.10 (s, 3H), 3.71-                                3.96 (m, 2H), 7.30 (d, 1H), 7.88 (dd, 1H), 7.96                                (d, 1H), 16.70 (s, 1H)                                                 3       IR (KBr Pellet): υ (cm.sup.-1) 3010, 2980, 2960,                       2900, 1690, 1600, 1580, 1560, 1410, 1310, 1150,                                1090, 970, 780, 760, 665                                                       MS (m/z): 55, 69, 84, 97, 138, 155, 217, 264,                                  279, 293, 303, 321, 349, 384 (M.sup.+), 386                            4       H-NMR (CDCl.sub.3): δ 1.55 (m, 1H), 2.07-2.60                            (m, 5H), 2.79 (m, 1H), 2.94 (t, 2H), 3.12 (s, 3H),                             3.15 (m, 1H), 7.39 (d, 1H), 7.87 (d, 2H), 7.94                                 (s, 1H), 16.72 (s, 1H)                                                         IR (Film): υ (cm.sup.-1), 3080, 3020, 2940, 2860,                      1680, 1580, 1550, 1400, 1320, 1150, 1090, 950, 830,                            770, 745, 660                                                                  MS: (m/z) 100, 113, 138, 155, 157, 217, 219, 224,                              226, 303, 305, 331, 365, 400 (M.sup.+)                                 5       H-NMR (CDCl.sub.3): 1.80 (m, 1H), 2.09 (m, 1H), 2.28                           (m, 2H), 2.67 (m, 2H), 2.80 (m, 1H), 3.12 (s, 3H),                             3.12 (m, 2H), 3.41 (m, 1H), 7.42 (d, 1H), 7.88                                 (dd, 1H), 7.98 (d, 1H), 16.8 (s, 1H)                                           IR (Film): υ (cm.sup.-1) 3060, 3020, 2960, 2930,                       1680, 1600, 1560, 1410, 1315, 1155, 1125, 960, 780,                            750, 730, 665                                                                  MS (m/z): 155, 157, 217, 219, 226, 264, 303, 305,                              317, 329, 397 (M.sup.+ -cl)                                            6       H-NMR (CDCl.sub.3): δ 1.63 (m, 1H), 1.85-(11214-32-0)                    2.30, (m, 5H), 2.77 (m, 1H), 3.03 (m, 1H), 3.77                                (m, 1H), 3.90 (m, 1H), 7.23 (d, 1H), 7.60 (t, 1H),                             7.71 (t, 1H), 8.21 (d, 1H), 16.57 (s, 1H)                                      IR (Film): υ (cm.sup.-1) 3100, 3000, 2960, 2900,                       1690, 1600, 1575, 1530, 1425, 1355                                             MS (m/z): 55, 69, 76, 84, 97, 150, 204, 214, 228,                              238, 256, 271, 317 (M.sup.+)                                           7       IR (KBr pellet): υ (cm.sup.-1) 3110, 11215-12-0)                       3070, 3000, 2970, 2900, 1690, 1610, 1580, 1550,                                1510, 1420, 1365, 1335, 1185, 1140, 1095.                                      MS (m/z): 55, 69, 84, 97, 125, 144, 218, 282, 339,                             366, 385 (M.sup.+)                                                     8       H-NMR (CDCl.sub.3): δ 1.54 (m, 1H), 2.00-2.50                            (m, 5H), 2.77 (m, 1H), 2.88 (m, 2H), 3.14 (m, 1H),                             7.41 (d, 1H), 7.95 (d, 1H), 8.48 (s, 1H), 16.22                                (s, 1H)                                                                        IR (film): υ (cm.sup.-1) 3090, 2940, 2860, 1670,                       1600, 1570, 1540, 1500, 1410, 1355, 1325, 1255,                                1180, 1155, 1135, 1085, 950, 920, 905, 890, 845,                               815, 790, 760, 700                                                             MS (m/z): 100, 113, 140, 218, 293, 338, 355, 401                               (M.sup.+)                                                              9       NMR (CDCl.sub.3): δ 1.75 (m, 1h), 2.00-2.35 (m, 3H),                     2.63 (m, 2h), 2.80 (m, 1H), 2.95-3.10 (m, 2H),                                 3.45 (m, 1H), 7.25 (d, 1H), 7.97 (d, 1H), 8.49                                 (s, 1H), 16.31 (s, 1H)                                                         IR (film): υ (cm.sup.-1) 3100, 3080, 2980, 2960, 2880,                 1675, 1600, 1580, 1540, 1450, 1430, 1360, 1330,                                1305, 1260, 118O, 1160, 1130, 1090, 955, 910, 850,                             820, 800, 770, 715, 700                                                        MS (m/z): 41, 43, 53, 55, 67, 69, 77, 79, 81, 126,                             133, 144, 146, 160, 172, 189, 198, 218, 226, 254,                              295, 307, 319, 387 (M.sup.+ - NO.sub.2), 414 (M.sup.+ - F)             11      NMR (CDCl.sub.3): δ 1.53 (m, 1H), 2.00-2.20 (m, 2H),                     2.35 (m, 1H), 2.47 (m, 2H), 2.79 (m, 1H), 2.88 (m,                             2H), 3.14 (m, 1H), 4.65 (s, 2H), 7.50 (d, 1H), 8.29                            (d, 1H), 8.78 (s, 1H) 16.02 (s, 1H)                                            IR (KBr pellet): υ (cm.sup.-1) 3100, 2940, 1670,                       1600, 1560, 1540, 1350, 1335, 1160, 890, 750                           12      NMR (CDCl.sub.3): δ 1.75 (m, 1H), 2.00-2.20 (m, 2H),                     2.32 (m, 1H), 2.62 (m, 2H), 2.82 (dd, 1H), 2.95-                               3.15 (m, 2H), 3.43 (m, 1H), 4.75 (s, 2H), 7.57                                 (d, 1H), 8.30 (d, 1H), 8.81 (s, 1H)                                            IR (KBr pellet): υ (cm.sup.-1) 3100, 3020, 2960,                       2880, 1680, 1610, 1570, 1540, 1420, 1360, 1340,                                1305, 1170, 1130, 900, 760, 730                                                MS (m/z): NH.sub.3 --DCI; 431 (M-NO.sub.2), 478 (MH.sup.+),                    495 (M.sup.+ NH.sub.4.sup.+),                                          ______________________________________                                    

Herbicidal Screening Tests

As previously mentioned, the herein described compounds produced in the above-described manner are phytotoxic compounds which are useful and valuable in controlling various plant species. Selected compounds of this invention were tested as herbicides in the following manner.

Pre-emergence herbicide test. On the day preceding treatment, seeds of nine different weed species are planted in loamy sand soil in individual rows using one species per row across the width of a flat. The seeds used are giant foxtail (FT) (Setaria faberi), watergrass (WG) (Echinochloa crusgalli), wild oat (WO) (Avena fatua), annual mornigglory (AMG) (Ipomoea lacunosa), velvetleaf (VL) (Abutilon theophrasti), yellow nutsedge (YNG) (Cyperus esculentus, broadleaf signalgrass (BSG) (Brachiaria platyphylla), cocklebur (CB) (Xanthium pensylvanicum) and sicklepod (SP) (Cassia obtusifolia). Ample seeds are planted to give about 20 to 40 seedlings per row, after emergence, depending upon the size of the plants.

Using an analytical balance, 37.5 milligrams (mg) of the compound to be tested are weighed out on a piece of glassine weighing paper. The paper and compound are placed in a 60 milliliter (ml) wide-mouth clear bottle and dissolved in 45 ml of acetone or substituted solvent. Eighteen ml of this solution are transferred to a 60 ml wide-mouth clear bottle and diluted with 22 ml of a water and acetone mixture (19:1) containing enough polyoxyethylene sorbitan monolaurate emulsifier to give a final solution of 0.5% (v/v). The solution is then sprayed on a seeded flat on a linear spray table calibrated to deliver 80 gallons per acre (748 L/ha). The application rate is 0.25 lb/acre (0.28 kg/ha).

After treatment, the flats are placed in the greenhouse at a temperature of 70° to 80° F. and watered by sprinkling. Two weeks after treatment, the degree of injury or control is determined by comparison with untreated check plants of the same age. The injury rating from 0 to 100% is recorded for each species as percent control with 0% representing no injury and 100% representing complete control.

The results of the tests are shown in the following Table II.

                  TABLE II                                                         ______________________________________                                         Pre-Emergence Multi-Weed Herbicide Test                                        Application Rate - 0.28 kg/ha                                                  Cmpd.                                                                          No.   FT     WG     WO   BSG  AMG   CB  VL   SP   YNS                          ______________________________________                                         1     50     30     40   0    20    0   60   30   0                            2     70     50     85   70   60    40  90   15   60                           3     40     90     0    20   70    --  100  20   80                           4     0      0      0    0    0     10  0    0    0                            5     10     80     0    0    20    --  100  20   30                           6     30     80     30   0    30    --  80   20   0                            7     100    100    20   100  80    --  100  0    --                           8     60     80     20   30   20    0   100  0    80                           9     100    100    90   100  100   --  100  95   80                           10    0      50     0    30   70    --  100  100  80                           11    0      0      10   0    0     --  0    50   0                            12    0      0      10   0    30    0   75   0    0                            ______________________________________                                          (--) = No Test Results                                                   

Post-Emergence Herbicide Test: This test is conducted in an identical manner to the testing procedure for the pre-emergence herbicide test, except the seeds of the nine different weed species are planted 10-12 days before treatment. Also, watering of the treated flats is confined to the soil surface and not to the foliage of the sprouted plants.

The results of the post-emergence herbicide test are reported in Table III.

                  TABLE III                                                        ______________________________________                                         Post-Emergence Multi-Weed Herbicide Test                                       Application Rate - 0.28 kg/ha                                                  Cmpd.                                                                          No.   FT     WG     WO   BSG  AMG   CB  VL   SP   YNS                          ______________________________________                                         1     100    60     75   80   30    70  100  20   0                            2     85     40     90   90   80    95  100  10   0                            3     80     85     0    0    85    90  100  40   30                           4     0      75     0    0    20    60  85   10   0                            5     65     90     0    0    50    85  80   10   0                            6     25     50     0    0    40    --  90   20   0                            7     80     60     10   30   80    --  100  40   10                           8     85     90     100  30   90    60  100  20   0                            9     90     90     90   80   90    80  100  80   0                            10    25     50     0    0    100   75  100  0    5                            11    0      0      0    0    30    20  10   0    0                            12    0      0      0    0    60    --  25   0    0                            ______________________________________                                          (--) No test results                                                     

The compounds of the present invention and their salts are useful as herbicides and can be applied in a variety of ways at various concentrations. In practice, the compounds or salts are formulated into herbicidal compositions, by admixture, in herbicidally effective amounts, with the adjuvants and carriers normally employed for facilitating the dispersion of active ingredients for agricultural applications, recognizing the fact that the formulation and mode of application of a toxicant may affect the activity of the materials in a given application. Thus, these active herbicidal compounds or salts can be formulated as granules of relatively large particle size, as wettable powders, as emulsifiable concentrates, as powdery dusts, as flowables, as solutions or as any of several other known types of formulations, depending upon the desired mode of application. These formulations may contain as little as about 0.5% to as much as about 95% or more by weight of active ingredient. A herbicidally effective amount depends upon the nature of the seeds or plants to be controlled and the rate of application varies from about 0.01 to approximately 10 pounds per acre, preferably from about 002 to about 4 pounds per acre.

Wettable powders are in the form of finely divided particles which disperse readily in water or other dispersants. The wettable powder is ultimately applied to the soil either as a dry dust or as a dispersion in water or other liquid. Typical carriers for wettable powders include fuller's earth, kaolin clays, silicas and other readily wet organic or inorganic diluents. Wettable powders normally are prepared to contain about 5% to about 95% of the active ingredient and usually also contain a small amount of wetting, dispersing, or emulsifying agent to facilitate wetting and dispersion.

Emulsifiable concentrates are homogeneous liquid compositions which are dispersible in water or other dispersant, and may consist entirely of the active compound or salt with a liquid or solid emulsifying agent, or may also contain a liquid carrier, such as xylene, heavy aromatic naphthal, isophorone and other non-volatile organic solvents. For herbicidal application, these concentrates are dispersed in water or other liquid carrier and normally applied as a spray to the area to be treated. The percentage by weight of the essential active ingredient may vary according to the manner in which the composition is to be applied, but in general comprises about 0.5% to 95% of active ingredient by weight of the herbicidal composition.

Granular formulations wherein the toxicant is carried on relatively coarse particles, are usually applied without dilution to the area in which suppression of vegetation is desired. Typical carriers for granular formulations include sand, fuller's earth, attapulgite clay, bentonite clays, montmorillonite clay, vermiculite, perlite and other organic or inorganic materials which absorb or which may be coated with the toxicant. Granular formulations normally are prepared to contain from about to about 25% of active ingredients which may include surface-active agents such as heavy aromatic naphthas, kerosene or other petroleum fractions, or vegetable oils; and/or stickers such as destrins, glue or synthetic resins.

Typical wetting, dispersing or emulsifying agents used in agricultural formulations include, for example, the alkyl and alkylaryl sulfonates and sulfates and their salts; polyhydric alcohols; polyethoxylated alcohols; esters and fatty amines; and other types of surface-active agents, many of which are available in commerce. The surface-active agent, when used, normally comprises from 0.1% to 15% by weight of the herbicidal composition.

Dusts, which are free-flowing admixtures of the active ingredient with finely divided solids such as talc, clays, flours and other organic and inorganic solids which act as dispersants and carriers for the toxicant, are useful formulations for soil-incorporating application.

Pastes, which are homogeneous suspensions of a finely divided solid toxicant in a liquid carrier such as water or oil, are employed for specific purposes. These formulations normally contain about 5% to about 95% of active ingredient by weight, and may also contain small amounts of a wetting, dispersing or emulsifying agent to facilitate dispersion. For application, the pastes are normally diluted and applied as a spray to the area to be affected.

Other useful formulations for herbicidal applications include simple solutions of the active ingredient in a dispersant in which it is completely soluble at the desired concentration, such as acetone, alkylated naphthalenes, xylene and other organic solvents. Pressurized sprays, typically aerosols, wherein the active ingredient is dispersed in finely-divided form as a result of vaporization of a low boiling dispersant solvent carrier, such as the Freons, may also be used.

The phytotoxic compositions of this invention can be applied to the plants in the conventional manner. Thus, the dust and liquid compositions can be applied to the plant by the use of power-dusters, boom and hand sprayers and spray dusters. The compositions can also be applied from airplanes as a dust or a spray or by rope wick applications because they are effective in very low dosages. In order to modify or control growth of germinating seeds or emerging seedlings, as a typical example, the dust and liquid compositions can be applied to the soil according to conventional methods and can be distributed in the soil to a depth of at least 1/2 inch below the soil surface. It is not necessary that the phytotoxic compositions be mechanically admixed with the soil particles since these compositions can also be applied merely by spraying or sprinkling the surface of the soil. The phytotoxic compositions of this invention can also be applied by addition to irrigation water supplied to the field to be treated. This method of application permits the penetration of the compositions into the soil as the water is absorbed therein. Dust compositions, granular compositions or liquid formulations applied to the surface of the soil can be distributed below the surface of the soil by conventional means such as discing, dragging or mixing operations. In the following examples the herbicidal compound can be substituted with the herbicidal salt of the compound.

    ______________________________________                                         EMULSIFIABLE CONCENTRATE FORMULATIONS                                          General Formula with Ranges                                                                    Specific Formula                                               ______________________________________                                         Herbicidal  5-55    herbicidal compound                                                                             24                                        compound                                                                       surfactant(s)                                                                              5-25    proprietary blend of oil-                                                                       10                                        solvent(s)  20-90   soluble sulfonates and                                                 100%    polyoxyethylene ethers                                                         polar solvent    27                                                            petroleum hydrocarbon                                                                           39                                                                             100%                                      WETTABLE POWDER FORMULATIONS                                                   herbicidal  3-90    herbicidal compound                                                                             80                                        compound                                                                       wetting agent                                                                              0.5-2   sodium dialkyl naphthalene                                                                      0.5                                       dispersing agent                                                                           1-8     sulfonate                                                  diluent(s)  8.5-87  sodium lignosulfonate                                                                           7                                                     100%    attapulgite clay 12.5                                                                           100%                                      EXTRUDED GRANULAR FORMULATIONS                                                 herbicidal  1-20    herbicidal compound                                                                             10                                        compound                                                                       binding agent                                                                              0-10    lignin sulfonate 5                                         diluent(s)  70-99   calcium carbonate                                                                               85                                                    100%                     100%                                      FLOWABLE FORMULATIONS                                                          herbicidal                                                                               20-70     herbicidal compound                                                                             45                                        compound                                                                       surfactant(s)                                                                             1-10     polyoxyethylene ether                                                                           5                                         suspending                                                                               0.05-1    attagel          0.05                                      agent(s)                                                                       antifreeze agent                                                                          1-10     propylene glycol 10                                        antimicrobial                                                                             1-10     1,2-benzisothiazoline-3-one                                                                     0.03                                      agent                                                                          antifoam agent                                                                           0.1-1     silicone defoamer                                                                               0.02                                      solvent   7.95-77.85                                                                               water            39.9                                                100%                       100%                                      ______________________________________                                    

When salts are used as the active ingredient in the herbicidal compositions of this invention it is recommended to use salts that are agriculturally acceptable.

The phytotoxic compositions of this invention can also contain other additives, for example, fertilizers, other herbicides and other pesticides, used as adjuvant or in combination with any of the above-described adjuvants. Fertilizers useful in combination with the active ingredients include, for example, ammonium nitrate, urea and superphosphate.

The herbicidal compounds of this invention can be used in combination with other herbicidal compounds for broader spectrum control of undesirable vegetation. Examples of other herbicidal compounds are as follows:

1. ANILIDES

Alachlor-2-chloro-2',6'-diethyl-N-(methoxymethyl)acetanilide

Metolachlor-2-chloro-N-(2-ethyl-6-methylphenyl)-N-(2-methoxy-1-methylethyl)acetamide

Propanil-N-(3,4-dichlorophenyl) propionanilide

2. TRIAZINES

Atrazine-2-chloro-4-(ethylamino)-6-(isopropylamino)-s-triazine

Cyanazine-2-chloro-4-(1-cyano-1-methylethylamino)-6-ethylamino-s-triazine

Metribuzin-4-amino-6-tert-butyl-3-(methylthio)-1,2,4-triazin-5(4H)-one

3. THIOCARBAMATES

Molinate-S-ethyl hexahydro-1H-azepine-1-carbothioate

Butylate-S-ethyl diisobutylthiocarbamate

4. UREAS

Monuron-3-(p-chlorophenyl)-1,1-dimethylurea

Linuron-3-(3,4-dichlorophenyl)-1-methoxy-1-methylurea

5. TOLUIDINES

Trifluralin-α, α, α-trifluoro-2,6-dinitro-N,N-dipropyl-p-toluidine

Pendimethalin-N-(1-ethylpropyl)-3,4-dimethyl-2,6-dinitrobenzenamine

6. HORMONES

2,4-D-(2,4-dichlorophenoxy) acetic acid

MCPA-(2-methyl-4-chlorophenoxy) acetic acid

7. DIAZINES

Bentazon-3-isopropyl-1H-2,3,1-benzothiadiazin-4(3H)-one 2,2-dioxide

Oxadiazon-2-tert-butyl-4-(2,4-dichloro-5-isopropoxyphenyl)-Δ² -1,3,4-oxadiazolin-5-one

8. DIPHENYL ETHERS

Acifluorfen-sodium 5-[2-chloro-4-(trifluoromethyl)phenyoxy]-2-nitrobenzoate

Fluazifop-butyl-(±)-butyl 2-[4[(5-(trifluoromethyl)-2-pyridinyl)oxy]phenoxy]propanoate

Chlomethoxynil-2,4-dichlorophenyl 3-methoxy-4-nitrophenyl ether

9. IMIDAZOLINONES

Imazaquin-2-(4,5-dihydro-4-methyl-4-(1-methylethyl)-5-oxo-1H-imidazol-2-yl)-3-quinolin carboxylic acid

10. SULFONYL UREAS

Bensulfuron methyl-methyl 2-((((((4,6-dimethoxypyrimidin-2-yl)-amino)carbonyl)amino)sulfonyl-1)methyl) benzoate

Chlorimuron ethyl-ethyl 2-(((((4-chloro-6-methoxypyrimidin-2-yl)amino)carbonyl)amino)sulfonyl)benzoate

11. MISCELLANEOUS COMPOUNDS

Dimethazone-2-(2-chlorophenyl)methyl-4,4-dimethyl-3-isoxazolidinone

Norflurazon-4-chloro-5-(methylamino)-2-(α, α, α-trifluoro-m-tolyl)-3-(2H)-pyridazinone

Dalapon-2,2-dichloropropionic acid

Glyphosate-isopropyl amine salt of N-(phosphonomethyl)glycine

Fenoxaprop-ethyl-(+)-ethyl-2,4-((6-chloro-2-benzoxazolyloxy)phenoxy) propanoate 

What is claimed is:
 1. Compounds of the formula ##STR19## wherein X is oxy, thio, sulfinyl or sulfonyl;R is halogen; C₁ -C₂ alkyl; C₁ -C₂ alkoxy; trifluoromethoxy; difluoromethoxy; nitro; cyano; C₁ -C₂ haloalkyl; R^(a) SO_(n) -- wherein n is 0 or 2 and R^(a) is C₁ -C₂ alkyl, trifluoromethyl or difluoromethyl; R¹ is hydrogen, C₁ -C₄ alkyl, phenyl or substituted phenyl; R² is hydrogen or C₁ -C₄ alkyl; or R¹ and R² together are C₂ -C₅ alkylene; R³ is hydrogen, C₁ -C₄ alkyl, phenyl or substituted phenyl with the proviso that R¹ and R³ are not both phenyl or substituted phenyl; R⁴ is hydrogen or C₁ -C₄ alkyl; and R⁵ and R⁶ independently are (1) hydrogen; (2) halogen; (3) C₁ -C₄ alkyl; (4) C₁ -C₄ alkoxy; (5) trifluoromethoxy; (6) cyano; (7) nitro; (8) C₁ -C₄ haloalkyl; (9) R^(b) SO_(n) -- wherein n is the integer 0, 1 or 2; and R^(b) is (a) C₁ -C₄ alkyl; (b) C₁ -C₄ alkyl substituted with halogen or cyano; (c) phenyl; or (d) benzyl; (10) --NR^(c) R^(d) wherein R^(c) and R^(d) independently are hydrogen or C₁ -C₄ alkyl; (11) R^(e) C(O)-- wherein R^(e) is C₁ -C₄ alkyl or C₁ -C₄ alkoxy; or (12) --SO₂ NR^(c) R^(d) wherein R^(c) and R^(d) are as defined; and (13) --N(R^(c))C(O)R^(d) wherein R^(c) and R^(d) are defined; and their salts.
 2. The compounds of claim 1 wherein R is chlorine, bromine, methyl, methoxy, nitro, trifluoromethyl or methylsulfonyl; R¹, R², R³ and R⁴ are hydrogen or methyl; R⁵ and R⁶ independently are (1) hydrogen; (2) C₁ -C₄ halogen; (3) C₁ -C₄ alkyl; (4) alkoxy; (5) trifluoromethoxy; (6) cyano; (7) nitro; (8) C₁ -C₄ haloalkyl; (9) R^(b) SO_(n) -- wherein n is the integer 0, 1 or 2; and R^(b) is (a) C₁ -C₄ alkyl; (b) C₁ -C₄ alkyl substituted with halogen or cyano; (c) phenyl; or (d) benzyl; (10)--NR^(c) R^(d) wherein R^(c) and R^(d) independently are hydrogen or C₁ -C₄ alkyl; (11) R^(e) C(O)-- wherein R^(e) is C₁ -C₄ alkyl or C₁ -C₄ alkoxy; or (12) SO₂ NR^(c) R^(d) wherein R^(c) and R^(d) are as defined; or (13) --N--(R^(c))C(O)R^(d) wherein R^(c) and R^(d) are as defined.
 3. The compounds of claim 2 wherein R⁵ and R⁶ are independently are hydrogen; chloride; fluorine; bromine; methyl; C₁ -C₄ alkoxy; trifluoromethoxy; cyano; nitro; trifluoromethyl; R^(b) SO_(n) -- wherein n is the integer 0 or 2 and R^(b) is methyl, chloromethyl, trifluoromethyl; ethyl or n-propyl, R^(e) C(O)-- where R^(e) is C₁ -C₄ alkyl; or SO₂ NR^(c) R^(d) wherein R^(c) and R^(d) are as defined, and R⁵ is in the 3-position and R⁶ is in the 4-position.
 4. The compounds of claim 2 wherein R⁵ is hydrogen and R⁶ are hydrogen, chlorine, bromine, fluorine, cyano, trifluoromethyl or R^(b) SO₂ wherein R^(b) is C₁ -C₄ alkyl or C₁ -C₄ haloalkyl.
 5. The compound of claim 2 wherein R is nitro; R¹ is hydrogen; R² is hydrogen; R³ is hydrogen; R⁴ is hydrogen; R⁵ is hydrogen; R⁶ is trifluoromethyl; and X is thio.
 6. The compound of claim 2 wherein R is nitro; R¹ is hydrogen; R² is hydrogen; R³ is hydrogen; R⁴ is hydrogen; R⁵ is hydrogen; R⁶ is trifluoromethyl; and X is sulfonyl.
 7. The compound of claim 2 wherein R is chlorine; R¹ is hydrogen; R² is hydrogen; R³ is hydrogen; R⁴ is hydrogen; R⁵ is hydrogen; R⁶ is 4--SO₂ CH₃ ; and X is thio.
 8. The compound of claim 2 wherein R is chlorine; R¹ is hydrogen; R² is hydrogen; R³ is hydrogen; R⁴ is hydrogen; R⁵ is hydrogen; R⁶ is 4--SO₂ CH₃ ; and X is sulfonyl.
 9. The compound of claim 2 wherein R is nitro; R¹ is hydrogen; R² is hydrogen; R³ is hydrogen; R⁴ is hydrogen; R⁵ is hydrogen; R⁶ is trifluoromethyl; and X is oxy.
 10. The compounds of claim 2 wherein R⁵ is hydrogen.
 11. The compounds of claim 3 wherein R⁵ is hydrogen.
 12. The method of controlling undesirable vegetation comprising applying to the area where control is desired, an herbicidally effective amount of a compound having the formula ##STR20## wherein X is oxy, thio, sulfinyl or sulfonyl;R is halogen; C₁ -C₂ alkyl; C₁ -C₂ alkoxy; trifluoromethoxy; difluoromethoxy; nitro; cyano; C₁ -C₂ haloalkyl; R^(a) SO_(n) -- wherein n is 0 or 2 and R^(a) is C₁ -C₂ alkyl; trifluoromethyl or difluoromethyl; R¹ is hydrogen, C₁ -C₄ alkyl, phenyl or substituted phenyl; R² is hydrogen or C₁ -C₄ alkyl; or R¹ and R² together are C₂ -C₅ alkylene; R³ is hydrogen, C₁ -C₄ alkyl with the proviso that R¹ and R³ are not both phenyl or substituted phenyl; R⁴ is hydrogen or C₁ -C₄ alkyl; and R⁵ and R⁶ independently are (1) hydrogen; (2) halogen; (3) C₁ -C₄ alkyl; (4) C₁ -C₄ alkoxy; (5) trifluoromethoxy; (6) cyano; (7) nitro; (8) C₁ -C₄ haloalkyl; (9) R^(b) SO_(n) -- wherein n is the integer 0, 1 or 2; and R^(b) is (a) C₁ -C₄ alkyl; (b) C₁ -C₄ alkyl substituted with halogen or cyano; (c) phenyl; or (d) benzyl; (10) --NR^(c) R^(d) wherein R^(c) and R^(d) independently are hydrogen or C₁ -C₄ alkyl; (11) R^(e) C(O)-- wherein R^(e) is C₁ -C₄ alkyl or C₁ -C₄ alkoxy; or (12) --SO₂ NR^(c) R^(d) wherein R^(c) and R^(d) are as defined; and (13) --N(R^(c))C(O)R^(d) wherein R^(c) and R^(d) are as defined; and their salts.
 13. The method of claim 12 wherein R is chlorine, bromine, methyl, methoxy, nitro, trifluoromethyl, or methylsulfonyl; R¹, R², R³ and R⁴ are hydrogen or methyl; R⁵ and R⁶ independently are (1) hydrogen; (2) halogen; (3) C₁ `C₄ alkyl; (4) C₁ -C₄ alkoxy; (5) trifluoromethoxy; (6) cyano; (7) nitro; (8) C₁ -C₄ haloalkyl; (9) R^(b) SO_(n) -- wherein n is the integer 0, 1 or 2; and R^(b) is (a) C₁ -C₄ alkyl; (b) C₁ `C₄ alkyl substituted with halogen or cyano; (c) phenyl; or (d) benzyl; (10) --NR^(c) R^(d) wherein R^(c) and R^(d) independently are hydrogen or C₁ -C₄ alkyl; (11) R^(e) C(O)-- wherein R^(e) is C₁ -C₄ alkyl or C₁ -C₄ alkoxy; or (12) SO₂ NR^(c) R^(d) wherein R^(c) and R^(d) are as defined; or (13) --N--(R^(c))C(O)R^(d) wherein R^(c) and R^(d) are as defined.
 14. The method of claim 13 wherein R⁵ and R⁶ are independently are hydrogen; chlorine; fluorine; bromine; methyl; C₁ -C₄ alkoxy; trifluoromethoxy; cyano; nitro; trifluoromethyl; R^(b) SO_(n) 13 wherein n is the integer 0 or 2 and R^(b) is methyl, chloromethyl, trifluoromethyl, ethyl, or n-propyl; R^(e) C(O)-- where R^(e) is C₁ -C₄ alkyl; or SO₂ NR^(c) R^(d) wherein R^(c) and R^(d) are as defined and R⁵ is in the 3-position and R⁶ is in the 4-position.
 15. The method of claim 13 wherein R⁵ is hydrogen, chlorine, bromine, fluorine, cyano, trifluoromethyl, or R^(b) SO₂ wherein R^(b) is C₁ -C₄ alkyl or C₁ -C₄ haloalkyl.
 16. The method of claim 12 wherein R is nitro; R¹ is hydrogen; R² is hydrogen; R³ is hydrogen; R⁴ is hydrogen; R⁵ is hydrogen; R⁶ is trifluoromethyl; and X is thio.
 17. The method of claim 12 wherein R is nitro; R¹ is hydrogen; R² is hydrogen; R³ is hydrogen; R⁴ is hydrogen; R⁵ is hydrogen; R⁶ is trifluoromethyl; and X is sulfonyl.
 18. The method of claim 12 wherein R is chlorine; R¹ is hydrogen; R² is hydrogen; R³ is hydrogen; R⁴ is hydrogen; R⁵ is hydrogen; R⁶ is 4-SO₂ CH₃ ; and X is thio.
 19. The method of claim 12 wherein R is chlorine; R¹ is hydrogen; R² is hydrogen; R³ is hydrogen; R⁴ is hydrogen; R⁵ is hydrogen; R⁶ is 4-SO₂ CH₃ ; and X is sulfonyl.
 20. The method of claim 12 wherein R is nitro; R¹ is hydrogen; R² is hydrogen; R³ is hydrogen; R⁴ is hydrogen; R⁵ is hydrogen; R⁶ is trifluoromethyl; and X is oxy.
 21. The method of claim 13 wherein R⁵ is hydrogen.
 22. The method of claim 14 wherein R⁵ is hydrogen.
 23. An herbicidal composition comprising an herbicidally active compound of the formula ##STR21## wherein X is oxy, thio, sulfinyl or sulfonyl;R is halogen; C₁ -C₂ alkyl; C₁ -C₂ alkoxy; trifluoromethoxy; difluoromethyxy; nitro; cyano; C₁ -C₂ haloakyl; R^(a) SO_(n) -- wherein n is 0 or 2 and R^(a) is C₁ -C₂ alkyl, trifluoromethyl or difluoromethyl; R¹ is hydrogen, C₁ -C₄ alkyl, phenyl or substituted phenyl; R² is hydrogen or C₁ -C₄ alkyl; or R¹ and R² together are C₂ -C₅ alkylene; R³ is hydrogen, C₁ -C₄ alkyl, phenyl or substituted phenyl with the proviso that R¹ and R³ are not both phenyl or substituted phenyl; R⁴ is hydrogen or C₁ -C₄ alkyl; and R⁵ and R⁶ independently are (1) hydrogen; (2) halogen; (3) C₁ -C₄ alkyl; (4) alkoxy; (5) trifluoromethoxy; (6) cyano; (7) nitro; (8) C₁ -C₄ haloakyl; (9) R^(b) SO_(n) -- wherein n is the integer 0, 1 or 2; and R^(b) is (a) C₁ -C₄ alkyl; (b) C₁ -C₄ alkyl substituted with halogen or cyano; (c) phenyl; or (d) benzyl; (10) --NR^(c) R^(d) wherein R^(c) and R^(d) independently are hydrogen or C₁ -C₄ alkyl; (11) R^(e) C(O)-- wherein R^(e) is C₁ -C₄ alkyl or C₁ -C₄ alkoxy; or (12) --SO₂ NR^(c) R^(d) wherein R^(c) and R^(d) are as defined; and (13) --N(R^(c))C(O)R^(d) wherein R^(c) and R^(d) are as defined; and their salts and an inert carrier therefor.
 24. The composition of claim 23 wherein R is chlorine, bromine, methyl, methoxy, nitro, trifluoromethyl or methylsulfonyl; R¹, R², R³ and R⁴ are hydrogen or methyl; R⁵ and R⁶ independently are (1) hydrogen; (2) halogen; (3) C₁ -C₄ alkyl; (4) C₁ -C₄ alkoxy; (5) trifluoromethoxy; (6) cyano; (7) nitro; (8) C₁ -C₄ haloalkyl; (9) R^(b) SO_(n) -- wherein n is the integer 0, 1 or 2; and R^(b) is (a) C₁ -C₄ alkyl; (b) C₁ -C₄ alkyl substituted with halogen or cyano; (c) phenyl; or (d) benzyl; (10) --NR^(c) R^(d) wherein R^(c) and R^(d) independently are hydrogen or C₁ -C₄ alkyl; (11) R^(e) C(O)-- wherein R^(e) is C₁ -C₄ alkyl or C₁ -C₄ alkoxy; or (12) SO₂ NR^(c) R^(d) wherein R^(c) and R^(d) are as defined; or (13) --N--(R^(c))C(O)R^(d) wherein R^(c) and R^(d) are as defined.
 25. The composition of claim 24 wherein R⁵ and R⁶ are independently are hydrogen; chlorine; fluorine; bromine; methyl; C₁ -C₄ alkoxy; trifluoromethoxy; cyano; nitro; trifluoromethyl; R^(b) SO_(n) -- wherein n is the integer 0 or 2 and R^(b) is methyl, chloromethyl, trifluoromethyl, ethyl, or n-propyl; R^(e) C(O)-- where R^(e) is C₁ -C₄ alkyl; or SO₂ NR^(c) R^(d) wherein R^(c) and R^(d) are as defined and R⁵ is in the 3-position and R⁶ is in the 4-position.
 26. The composition of claim 24 wherein R⁵ is hydrogen and R⁶ is hydrogen, chlorine, bromine, fluorine, cyano, trifluoromethy or R^(b) SO₂ wherein R^(b) is C₁ -C₄ alkyl or C₁ -C₄ haloalkyl.
 27. The composition of claim 24 wherein R is nitro; R¹ is hydrogen; R² is hydrogen; R³ is hydrogen; R⁴ is hydrogen; R⁵ is hydrogen; R⁶ is trifluoromethyl; and X is thio.
 28. The composition of claim 24 wherein R is nitro; R¹ is hydrogen; R² is hydrogen; R³ is hydrogen; R⁴ is hydrogen; R⁵ is hydrogen; R⁶ is trifluoromethyl; and X is sulfonyl.
 29. The composition of claim 24 wherein R is chlorine; R¹ is hydrogen; R² is hydrogen; R³ is hydrogen; R⁴ is hydrogen; R⁵ is hydrogen; R⁶ is 4-SO₂ CH₃ ; and X is thio.
 30. The composition of claim 24 wherein R is chlorine; R¹ is hydrogen; R² is hydrogen; R³ is hydrogen; R⁴ is hydrogen; R⁵ is hydrogen; R⁶ is 4-SO₂ Ch₃ ; and X is sulfonyl.
 31. The composition of claim 25 wherein R is nitro; R¹ is hydrogen; R² is hydrogen; R³ is hydrogen; R⁴ is hydrogen; R⁵ is hydrogen; R⁶ is trifluoromethyl; and X is oxy.
 32. A compound of the structural formula ##STR22## wherein X is oxy, thio, sulfinyl or sulfonyl;R is halogen; C₁ -C₂ alkyl; C₁ -C₂ alkoxy; trifluoromethoxy; difluoromethoxy; nitro; cyano; C₁ -C₂ haloalkyl; R^(a) SO_(n) -- wherein n is 0 or 2 and R^(a) is C₁ -C₂ alkyl; trifluoromethyl or difluoromethyl; R¹ is hydrogen, C₁ -C₄ alkyl, phenyl or substituted phenyl; R² is hydrogen or C₁ -C₄ alkyl; or R¹ and R² together are C₂ -C₂ alkylene; R³ is hydrogen, C₁ -C₄ alkyl, phenyl or substituted phenyl with the proviso that R¹ and R³ are not both phenyl or substituted phenyl; R⁴ is hydrogen or C₁ -C₄ alkyl; and R⁵ and R⁶ independently are (1) hydrogen; (2) halogen; (3) (4) C₁ -C₄ alkoxy; C₁ -C₄ alkyl; (5) trifluoromethoxy; (6) cyano; (7) nitro; (8) C₁ -C₄ haloalkyl; (9) R^(b) SO_(n) -- wherein n is the integer 0, 1 or 2; and R^(b) is (a) C₁ -C₄ alkyl; (b) C₁ -C₄ alkyl substituted with halogen or cyano; (c) phenyl; or (d) benzyl; (10) --NR^(c) R^(d) wherein R^(c) and R^(d) independently are hydrogen or C₁ -C₄ alkyl; (11) R^(e) C(O)-- wherein R^(e) is C₁ -C₄ alkyl or C₁ -C₄ alkoxy; or (12) --SO₂ NR^(c) R^(d) wherein R^(c) and R^(d) are as defined; and (13) --N(R^(c))C(O)R^(d) wherein R^(c) and R^(d) are as defined. 